Expression of Flt3-ligand by the endothelial cell

被引:49
作者
Solanilla, A
Grosset, C
Lemercier, C
Dupouy, M
Mahon, FX
Schweitzer, K
Reiffers, J
Weksler, B
Ripoche, J
机构
[1] Univ Bordeaux 2, F-33076 Bordeaux, France
[2] Free Univ Amsterdam Hosp, Dept Hematol, Amsterdam, Netherlands
[3] Cornell Univ, Med Ctr, New York Hosp, Dept Med, New York, NY 10021 USA
关键词
Flt3-ligand; endothelial cell; hematopoiesis;
D O I
10.1038/sj.leu.2401635
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Flt3-ligand (FL) is a cytokine that is of paramount importance in the proliferation of primitive hematopoietic progenitors. In this study, we show that endothelial cells (EC) produce large amounts of soluble FL and express a membrane-bound form of the molecule. Bone marrow microvascular EC also produce FL, suggesting that EC are an important source of FL in the bone marrow. High concentrations of FL in EC supernatants contrast with its undetectable levels in long-term bone marrow cultures. A single mRNA for FL is detected, suggesting that soluble FL derives from the membrane-bound species by proteolytic release. FL mRNA is stable with a half-life of about 3 h. II-1 alpha increases FL mRNA levels and membrane and soluble FL expression. Glucocorticoids, known inhibitors for many hematopoietic growth factors do not down-regulate the expression of FL. On the contrary, GC increase the expression of both species of FL. The neutralization of FL in cocultures EC/hematopoietic progenitors results in an acceleration of the maturation of the progenitors. IFN-alpha, MIP-1 alpha and TGF-beta stimulate production of membrane-bound and soluble FL. This stimulation is essential to explain their modulatory effect on the generation of clonogenic cells in cocultures EC/hematopoietic progenitors.
引用
收藏
页码:153 / 162
页数:10
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